FDA Medical Device Recalls (openFDA)
Handicare Usa Inc: Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
- Recall number
- Z-2753-2018
- Recalling firm
- Handicare Usa Inc
- Product
- Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
- Status
- Terminated
- Initiated
- 2017-11-03
- Posted
- not on file
- Terminated
- 2020-07-10
- Reason
- Premature strap wear and breakage at maximum weight conditions (625 lbs.).
- Root cause
- Nonconforming Material/Component
- Action
- HandiCare USA sent an Urgent notification letter dated November 3, 2017 to their customers. The letter identified the affected product, problem and actions to be taken. Customers were informed new units will be sent to replace the affected units identified at no charge. For questions contact your Customer Service
- Quantity
- 4
- Distribution
- Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,
- Lot, serial or model codes
- Device Model; 303090 and 303093
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- Firm FEI
- 3007802293
- Firm city
- Maryland Heights
- Firm state
- MO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28